Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10226620
rs10226620
Entrez Id: 7975;202915
Gene Symbol: MAFK;TMEM184A
MAFK;TMEM184A
CUI: C0740651
Disease:
Abdominal symptom 		0.010 GeneticVariation BEFREE This case control study examined the associations between <i>MAFK</i> single nucleotide polymorphisms (rs4268033 G>A, rs3735656 T>C and rs10226620 C>T) and ulcerative colitis susceptibility in 174 patients with ulcerative colitis (UC) cases, and 748 subjects without no lower abdominal symptoms, diarrhea or hematochezia (controls). 28839436 2017
dbSNP: rs10226620
rs10226620
Entrez Id: 7975;202915
Gene Symbol: MAFK;TMEM184A
MAFK;TMEM184A
CUI: C0009324
Disease:
Ulcerative Colitis 		0.010 GeneticVariation BEFREE There was no significant association between rs10226620 and ulcerative colitis. 28839436 2017
dbSNP: rs10226620
rs10226620
Entrez Id: 7975;202915
Gene Symbol: MAFK;TMEM184A
MAFK;TMEM184A
CUI: C0018932
Disease:
Hematochezia 		0.010 GeneticVariation BEFREE This case control study examined the associations between <i>MAFK</i> single nucleotide polymorphisms (rs4268033 G>A, rs3735656 T>C and rs10226620 C>T) and ulcerative colitis susceptibility in 174 patients with ulcerative colitis (UC) cases, and 748 subjects without no lower abdominal symptoms, diarrhea or hematochezia (controls). 28839436 2017
dbSNP: rs10226620
rs10226620
Entrez Id: 7975;202915
Gene Symbol: MAFK;TMEM184A
MAFK;TMEM184A
CUI: C1321898
Disease:
Blood in stool 		0.010 GeneticVariation BEFREE This case control study examined the associations between <i>MAFK</i> single nucleotide polymorphisms (rs4268033 G>A, rs3735656 T>C and rs10226620 C>T) and ulcerative colitis susceptibility in 174 patients with ulcerative colitis (UC) cases, and 748 subjects without no lower abdominal symptoms, diarrhea or hematochezia (controls). 28839436 2017
dbSNP: rs4268033
rs4268033
Entrez Id: 202915
Gene Symbol: TMEM184A
TMEM184A
CUI: C0009324
Disease:
Ulcerative Colitis 		0.010 GeneticVariation BEFREE In particular, rs4268033 is closely associated with an increased risk for the development of UC. 28839436 2017